Prescription drug · ANDA
Finasteride NDC 71205-790
Finasteride 1 mg/1 · Tablet, Coated · Oral · Proficient Rx LP
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71205-790-30 | 71205079030 | 30 TABLET, COATED in 1 BOTTLE (71205-790-30)Marketed from Apr 17, 2023 | |
| 71205-790-60 | 71205079060 | 60 TABLET, COATED in 1 BOTTLE (71205-790-60)Marketed from Apr 17, 2023 | |
| 71205-790-90 | 71205079090 | 90 TABLET, COATED in 1 BOTTLE (71205-790-90)Marketed from Apr 17, 2023 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Finasteride
- Generic name (nonproprietary)
- finasteride
- Active ingredients
- Finasteride — 1 mg/1
- Dosage form
- Tablet, Coated
- Route
- Oral
- Labeler
- Proficient Rx LP
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 207750
- Marketing start
- Listing expires
- Other FDA classes
- 5-alpha Reductase Inhibitors (Mechanism)
- Identifiers
- Product ID 71205-790_196f7d23-ed90-46c2-ae34-615e6ec1650bSPL ID 196f7d23-ed90-46c2-ae34-615e6ec1650bSPL set ID 196f7d23-ed90-46c2-ae34-615e6ec1650bRxCUI 200172UNII 57GNO57U7GUPC 0371205790301
- Pharmacologic class
- 5-alpha Reductase Inhibitor
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N471205079030followed by a unit qualifier and the quantityPackage 71205-0790-30. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Finasteride tablets is indicated for the treatment of male pattern hair loss (androgenetic alopecia) in MEN ONLY . Efficacy in bitemporal recession has not been established. Finasteride tablets is not indicated for use in women. • Finasteride tablets is a 5α-reductase inhibitor indicated for the treatment of male pattern hair loss (androgenetic alopecia) in MEN ONLY ( 1 ). • Finasteride tablets is not indicated for use in women ( 1 , 4 , 5.1 ).
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 207750
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Finasteride | Finasteride 1 mg/1 | Tablet, CoatedOral | Bryant Ranch Prepack | 71335-1304 |
| Finasteride | Finasteride 1 mg/1 | Tablet, CoatedOral | Ascend Laboratories, LLC | 67877-455 |
| Finasteride | Finasteride 1 mg/1 | Tablet, CoatedOral | A-S Medication Solutions | 50090-4648 |
| Finasteride | Finasteride 1 mg/1 | Tablet, CoatedOral | REMEDYREPACK INC. | 70518-2287 |
| Finasteride | Finasteride 1 mg/1 | Tablet, CoatedOral | Preferred Pharmaceuticals Inc. | 68788-8275 |
| Finasteride | Finasteride 1 mg/1 | TabletOral | Thirty Madison Inc | 71713-099 |
| Finasteride | Finasteride 1 mg/1 | Tablet, CoatedOral | NuCare Pharmaceuticals, Inc. | 68071-3744 |